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rs201096554

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201096554(C;T)
Make rs201096554(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89530785
GeneSPG7
is asnp
is mentioned by
dbSNPrs201096554
ClinGenrs201096554
ebirs201096554
HLIrs201096554
Exacrs201096554
Varsomers201096554
Maprs201096554
PheGenIrs201096554
hapmaprs201096554
1000 genomesrs201096554
hgdprs201096554
ensemblrs201096554
gopubmedrs201096554
geneviewrs201096554
scholarrs201096554
googlers201096554
pharmgkbrs201096554
gwascentralrs201096554
openSNPrs201096554
23andMers201096554
23andMe allrs201096554
SNP Nexus

SNPshotrs201096554
SNPdbers201096554
MSV3drs201096554
GWAS Ctlgrs201096554
Max Magnitude0
ClinVar
Risk rs201096554(T;T)
Alt rs201096554(T;T)
Reference Rs201096554(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPG7
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89597193C>T
CLNSRC
CLNACC RCV000198540.1,